![Analysis of the Association Between Adverse Events and Outcome in Patients Receiving a Programmed Death Protein 1 or Programmed Death Ligand 1 Antibody | Journal of Clinical Oncology Analysis of the Association Between Adverse Events and Outcome in Patients Receiving a Programmed Death Protein 1 or Programmed Death Ligand 1 Antibody | Journal of Clinical Oncology](https://ascopubs.org/na101/home/literatum/publisher/asco/journals/content/jco/2019/jco.2019.37.issue-30/jco.19.00318/20191004/images/large/jco.19.00318ta4.jpeg)
Analysis of the Association Between Adverse Events and Outcome in Patients Receiving a Programmed Death Protein 1 or Programmed Death Ligand 1 Antibody | Journal of Clinical Oncology
Guide for Surveillance of Adverse Events of Special Interest (AESI) during novel Oral Polio Vaccine type 2 (nOPV2) Use
![Challenges in conducting post-authorisation safety studies (PASS): A vaccine manufacturer's view - ScienceDirect Challenges in conducting post-authorisation safety studies (PASS): A vaccine manufacturer's view - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0264410X17305509-gr1.jpg)
Challenges in conducting post-authorisation safety studies (PASS): A vaccine manufacturer's view - ScienceDirect
![Safety analyses from the phase 3 ASCENT trial of sacituzumab govitecan in metastatic triple-negative breast cancer | npj Breast Cancer Safety analyses from the phase 3 ASCENT trial of sacituzumab govitecan in metastatic triple-negative breast cancer | npj Breast Cancer](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs41523-022-00467-1/MediaObjects/41523_2022_467_Fig1_HTML.png)
Safety analyses from the phase 3 ASCENT trial of sacituzumab govitecan in metastatic triple-negative breast cancer | npj Breast Cancer
![Ministry of Health on Twitter: "#Unite2FightCorona #LargestVaccineDrive DCGI approves “Conditional Market Authorization” of two #COVID19 Vaccines- Covaxin and Covishield. https://t.co/kpDLdyYm48 https://t.co/fr5kMQv2OZ" / Twitter Ministry of Health on Twitter: "#Unite2FightCorona #LargestVaccineDrive DCGI approves “Conditional Market Authorization” of two #COVID19 Vaccines- Covaxin and Covishield. https://t.co/kpDLdyYm48 https://t.co/fr5kMQv2OZ" / Twitter](https://pbs.twimg.com/media/FKGy-gzVkAMs2bN.jpg)
Ministry of Health on Twitter: "#Unite2FightCorona #LargestVaccineDrive DCGI approves “Conditional Market Authorization” of two #COVID19 Vaccines- Covaxin and Covishield. https://t.co/kpDLdyYm48 https://t.co/fr5kMQv2OZ" / Twitter
![Adverse Events in Giant Cell Arteritis and Rheumatoid Arthritis Patient Populations: Analyses of Tocilizumab Clinical Trials and Claims Data | SpringerLink Adverse Events in Giant Cell Arteritis and Rheumatoid Arthritis Patient Populations: Analyses of Tocilizumab Clinical Trials and Claims Data | SpringerLink](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs40744-019-0139-5/MediaObjects/40744_2019_139_Fig1_HTML.png)
Adverse Events in Giant Cell Arteritis and Rheumatoid Arthritis Patient Populations: Analyses of Tocilizumab Clinical Trials and Claims Data | SpringerLink
![Cumulation of Safety Data from a Randomized Clinical Trial, the AESI is... | Download Scientific Diagram Cumulation of Safety Data from a Randomized Clinical Trial, the AESI is... | Download Scientific Diagram](https://www.researchgate.net/profile/Jiabu-Ye/publication/340101520/figure/tbl1/AS:897466505363457@1590984097842/Cumulation-of-Safety-Data-from-a-Randomized-Clinical-Trial-the-AESI-is-Myocardial.png)
Cumulation of Safety Data from a Randomized Clinical Trial, the AESI is... | Download Scientific Diagram
Guide for Surveillance of Adverse Events of Special Interest (AESI) during Novel Oral Polio Vaccine Type 2 (nOPV2) Use
![Primary results of STRONG: An open-label, multicenter, phase 3b study of fixed-dose durvalumab monotherapy in previously treated patients with urinary tract carcinoma - European Journal of Cancer Primary results of STRONG: An open-label, multicenter, phase 3b study of fixed-dose durvalumab monotherapy in previously treated patients with urinary tract carcinoma - European Journal of Cancer](https://els-jbs-prod-cdn.jbs.elsevierhealth.com/cms/attachment/a2584eb8-da36-408b-8602-8f6ad1fa3657/ga1_lrg.jpg)
Primary results of STRONG: An open-label, multicenter, phase 3b study of fixed-dose durvalumab monotherapy in previously treated patients with urinary tract carcinoma - European Journal of Cancer
![Protocol for a double-blind, randomized controlled trial on the dose-related efficacy of omalizumab in multi-food oral immunotherapy | Allergy, Asthma & Clinical Immunology | Full Text Protocol for a double-blind, randomized controlled trial on the dose-related efficacy of omalizumab in multi-food oral immunotherapy | Allergy, Asthma & Clinical Immunology | Full Text](https://media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs13223-020-00419-z/MediaObjects/13223_2020_419_Fig4_HTML.png)
Protocol for a double-blind, randomized controlled trial on the dose-related efficacy of omalizumab in multi-food oral immunotherapy | Allergy, Asthma & Clinical Immunology | Full Text
![Analysis of the Association Between Adverse Events and Outcome in Patients Receiving a Programmed Death Protein 1 or Programmed Death Ligand 1 Antibody | Journal of Clinical Oncology Analysis of the Association Between Adverse Events and Outcome in Patients Receiving a Programmed Death Protein 1 or Programmed Death Ligand 1 Antibody | Journal of Clinical Oncology](https://ascopubs.org/na101/home/literatum/publisher/asco/journals/content/jco/2019/jco.2019.37.issue-30/jco.19.00318/20191004/images/large/jco.19.00318ta1.jpeg)
Analysis of the Association Between Adverse Events and Outcome in Patients Receiving a Programmed Death Protein 1 or Programmed Death Ligand 1 Antibody | Journal of Clinical Oncology
![Adverse Events of Special Interest, SLE Medication Utilization, Hospitalizations, and Organ Damage: Results from a Phase 4, Randomized, Double-Blind, Placebo-Controlled, 52-week Study of Belimumab in Adults with Active, Autoantibody-Positive SLE - ACR Adverse Events of Special Interest, SLE Medication Utilization, Hospitalizations, and Organ Damage: Results from a Phase 4, Randomized, Double-Blind, Placebo-Controlled, 52-week Study of Belimumab in Adults with Active, Autoantibody-Positive SLE - ACR](https://acrabstracts.org/wp-content/uploads/2019/08/GTUOHVCE-697556-1-ANY-1-.png)